Skip to main content
OpenTrials
Completed

NCT Number: NCT02760290

Comparison of Extraperitoneal and Intraperitoneal Cesarean Technique

Cesarean section will performed via intraperitoneally and extraperitoneally. During postoperative period pain, need for analgesia, respiratory function tests, ileus, bowel movement, discharged time will be compared.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Postpartum Fever Digestive System Diseases Female Urogenital Diseases and Pregnancy Complications Gastrointestinal Diseases Hemorrhage Ileus Infections Intestinal Diseases Intestinal Obstruction Neurologic Manifestations Pain Pathologic Processes Pathological Conditions, Signs and Symptoms Pregnancy Complications Pregnancy Complications, Infectious Puerperal Disorders Puerperal Infection Signs and Symptoms Urogenital Diseases

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Zeynep Kamil Maternity and Pediatric Research and Training Hospital

Istanbul, 34668, Turkey (Türkiye)

About this study

Investigators will compared results intra and extraperitoneal cesarean section. Two groups will determine according to random numbers table. After operations, blood count, C reactive proteins, postoperative temperature, need for analgesia, ileus, bowel movement, mobilization time will compare by blind physician. Abdominal, shoulder and incisional pain at postoperative 0, 6, 12, 18, 24, 30 hours will compared by use visual analog score. Neonatal results and complications also will compare. Investigators and participants will be blind regarding technique.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Cesarean section for any reasons

Exclusion criteria

  • Involuntary

Treatment and study plan

Extraperitoneal cesarean section

Procedure

Intraperitoneal cesarean section

Procedure

Primary outcomes

  1. Pain Scores as measured by the Visual Analog Scale

    Time frame: 2 days

Secondary outcomes

  1. Blood count

    Time frame: 2 days

  2. C reactive proteins level

    Time frame: 2 days

  3. Complications

    Time frame: 2 days

  4. Discharge time

    Time frame: 4 days

  5. Forced expiratory volume in 1 second

    Time frame: 2 days

  6. Forced vital capacity

    Time frame: 2 days

  7. Peak expiratory flow

    Time frame: 2 days

Sponsors and collaborators

Lead sponsor

Zeynep Kamil Maternity and Pediatric Research and Training Hospital

Other

Registry information

Official study title

Comparison of Extraperitoneal and Intraperitoneal Cesarean Technique: Double Blind Controlled Study

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
May 3, 2016
Registry last updated
Mar 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.